Job Description:
This position functions as a member of the Biostatistics and Statistical Programming project team supporting the Lead Statistical Programmer in the development of programs to support the conduct statistical analysis and reporting of projects. A Statistical Programmer I creates, tests and maintains programs for clinical studies, under the direction of more senior programmers. He or she participates in the creation and maintenance of Statistical Programming project documentation.
• Uses SAS to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications.
• Works to ensure that outputs meet quality standards and project requirements.
• Performs validation programming and works with other Statistical Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.
• Keeps project team members informed of programming progress and issues requiring their attention.
• Follows applicable SOPs and relevant regulatory guidelines (e.g. ICH).
• Maintains well organized, complete, and up-to-date project documentation, and verification/quality control documents and programs, ensuring inspection readiness.
• Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.
• Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.
• Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
• Completes project programming activities within timeframe allotted by Lead Statistical Programmer and/or management.
• Performs other work-related duties as assigned.
• Minimal travel may be required.
• Works to ensure that outputs meet quality standards and project requirements.
• Performs validation programming and works with other Statistical Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.
• Keeps project team members informed of programming progress and issues requiring their attention.
• Follows applicable SOPs and relevant regulatory guidelines (e.g. ICH).
• Maintains well organized, complete, and up-to-date project documentation, and verification/quality control documents and programs, ensuring inspection readiness.
• Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.
• Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.
• Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
• Completes project programming activities within timeframe allotted by Lead Statistical Programmer and/or management.
• Performs other work-related duties as assigned.
• Minimal travel may be required.
• Undergraduate Degree, preferably in a scientific or statistical discipline; In lieu of degree, an equivalent combination of education and demonstrated programming experience.
• Proficiency in programming in SAS preferably in a clinical trial environment.
• Excellent written and verbal communication skills.
• Ability to read, write, speak, and understand English.
– Send us your resume
– Vacancy of interest:
• Proficiency in programming in SAS preferably in a clinical trial environment.
• Excellent written and verbal communication skills.
• Ability to read, write, speak, and understand English.
– Send us your resume
– Vacancy of interest: